NHERF1 (NHERF family PDZ scaffold protein 1) - Rat Genome Database

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Gene: NHERF1 (NHERF family PDZ scaffold protein 1) Homo sapiens
Analyze
Symbol: NHERF1
Name: NHERF family PDZ scaffold protein 1
RGD ID: 1342625
HGNC Page HGNC:11075
Description: Enables several functions, including PDZ domain binding activity; channel regulator activity; and signaling receptor binding activity. Involved in several processes, including establishment of Golgi localization; establishment or maintenance of epithelial cell apical/basal polarity; and regulation of signal transduction. Located in apical plasma membrane; microvillus; and perinuclear region of cytoplasm. Implicated in hypophosphatemic nephrolithiasis/osteoporosis 2.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: EBP50; ezrin-radixin-moesin binding phosphoprotein-50; ezrin-radixin-moesin-binding phosphoprotein 50; Na(+)/H(+) exchange regulatory cofactor 1; Na(+)/H(+) exchange regulatory cofactor NHE-RF1; Na+/H+ exchange regulatory co-factor; NHE-RF; NHERF; NHERF-1; NPHLOP2; regulatory cofactor of Na(+)/H(+) exchanger; SLC9A3 regulator 1; SLC9A3R1; sodium-hydrogen exchanger regulatory factor 1; sodium/hydrogen exchanger regulatory factor 1; solute carrier family 9 (sodium/hydrogen exchanger), isoform 3 regulator 1; solute carrier family 9 (sodium/hydrogen exchanger), isoform 3 regulatory factor 1; solute carrier family 9 (sodium/hydrogen exchanger), member 3 regulator 1; solute carrier family 9 isoform A3 regulatory factor 1; solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3 regulator 1
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381774,748,628 - 74,769,353 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1774,748,628 - 74,769,353 (+)EnsemblGRCh38hg38GRCh38
GRCh371772,744,767 - 72,765,492 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361770,256,373 - 70,277,089 (+)NCBINCBI36Build 36hg18NCBI36
Build 341770,256,378 - 70,277,089NCBI
Celera1769,337,944 - 69,358,679 (+)NCBICelera
Cytogenetic Map17q25.1NCBI
HuRef1768,155,124 - 68,175,866 (+)NCBIHuRef
CHM1_11772,809,571 - 72,830,338 (+)NCBICHM1_1
T2T-CHM13v2.01775,640,506 - 75,661,228 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(1->4)-beta-D-glucan  (ISO)
1,2-dibromoethane  (ISO)
1,2-dimethylhydrazine  (ISO)
1,4-dioxane  (ISO)
14-Deoxy-11,12-didehydroandrographolide  (EXP)
17alpha-ethynylestradiol  (EXP,ISO)
17beta-estradiol  (EXP,ISO)
2,2',4,4'-Tetrabromodiphenyl ether  (EXP)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2,4,6-tribromophenol  (EXP)
2-methylcholine  (EXP)
2-nitrotoluene  (ISO)
3,3',4,4',5-pentachlorobiphenyl  (ISO)
3,3',4,4'-tetrachlorobiphenyl  (ISO)
3,3',5,5'-tetrabromobisphenol A  (EXP)
3,4-methylenedioxymethamphetamine  (ISO)
4,4'-sulfonyldiphenol  (ISO)
4-hydroxyphenyl retinamide  (ISO)
5-aza-2'-deoxycytidine  (ISO)
6-propyl-2-thiouracil  (ISO)
acetonitrile  (ISO)
acrolein  (EXP)
Aflatoxin B2 alpha  (EXP)
all-trans-retinoic acid  (EXP)
alpha-pinene  (EXP)
ammonium chloride  (ISO)
arsane  (EXP)
arsenic atom  (EXP)
arsenous acid  (EXP)
benzene  (ISO)
benzo[a]pyrene  (EXP,ISO)
benzo[e]pyrene  (EXP)
bisphenol A  (EXP,ISO)
bisphenol F  (ISO)
bleomycin A2  (ISO)
bromobenzene  (ISO)
C60 fullerene  (ISO)
cadmium dichloride  (ISO)
caffeine  (EXP)
captan  (ISO)
carbon nanotube  (ISO)
cisplatin  (EXP)
clofibrate  (ISO)
clofibric acid  (ISO)
copper atom  (EXP,ISO)
copper(0)  (EXP,ISO)
copper(II) sulfate  (EXP)
coumarin  (EXP)
coumestrol  (EXP)
crocidolite asbestos  (EXP)
Cuprizon  (ISO)
cyclosporin A  (EXP)
cypermethrin  (ISO)
cytarabine  (EXP)
decabromodiphenyl ether  (EXP)
deoxynivalenol  (ISO)
diarsenic trioxide  (EXP)
diclofenac  (ISO)
diethyl maleate  (ISO)
diethylstilbestrol  (ISO)
dioxygen  (EXP)
diuron  (EXP,ISO)
doxorubicin  (EXP)
endosulfan  (ISO)
Enterolactone  (EXP)
enzyme inhibitor  (EXP)
epoxiconazole  (ISO)
ethanol  (ISO)
etoposide  (ISO)
flavonoids  (ISO)
fluoranthene  (ISO)
folic acid  (ISO)
folpet  (ISO)
FR900359  (EXP)
furan  (ISO)
genistein  (EXP,ISO)
gentamycin  (ISO)
glafenine  (ISO)
glycidol  (ISO)
hydrogen peroxide  (EXP)
inulin  (ISO)
ivermectin  (EXP)
leflunomide  (ISO)
lipopolysaccharide  (EXP)
methamphetamine  (ISO)
methapyrilene  (EXP)
methylmercury chloride  (EXP)
methylmercury(1+)  (ISO)
N-nitrosodiethylamine  (ISO)
nickel atom  (EXP)
ozone  (EXP)
paracetamol  (ISO)
perfluorooctane-1-sulfonic acid  (ISO)
phenobarbital  (ISO)
piperonyl butoxide  (ISO)
pirinixic acid  (ISO)
potassium dichromate  (EXP)
progesterone  (EXP)
quercetin  (EXP)
raloxifene  (EXP)
rotenone  (ISO)
S-(1,2-dichlorovinyl)-L-cysteine  (EXP)
Salmeterol xinafoate  (EXP)
SB 431542  (EXP)
sodium arsenite  (ISO)
tamibarotene  (EXP)
tamoxifen  (ISO)
temozolomide  (EXP)
tetrachloroethene  (ISO)
tetrachloromethane  (ISO)
tetraphene  (ISO)
titanium dioxide  (EXP,ISO)
toluene  (ISO)
Tributyltin oxide  (ISO)
trichloroethene  (ISO)
triclosan  (EXP)
trovafloxacin  (ISO)
urethane  (EXP,ISO)
valproic acid  (EXP)
vinclozolin  (ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process
actin cytoskeleton organization  (IEA,ISO)
adenylate cyclase-activating dopamine receptor signaling pathway  (IEA,ISO)
auditory receptor cell stereocilium organization  (IEA,ISO)
bile acid secretion  (IEA,ISS)
cerebrospinal fluid circulation  (IEA,ISS)
cilium organization  (IEA,ISS)
establishment of epithelial cell apical/basal polarity  (IMP)
establishment of Golgi localization  (IMP)
establishment of localization in cell  (IEA,ISO)
fibroblast migration  (IEA,ISO)
gamma-aminobutyric acid import  (IEA,ISS)
gland morphogenesis  (IMP)
glutathione transport  (IEA,ISS)
import across plasma membrane  (IEA,ISS)
intracellular phosphate ion homeostasis  (IEA,ISO)
maintenance of epithelial cell apical/basal polarity  (IEA,IMP,ISS)
microvillus assembly  (IMP)
morphogenesis of an epithelium  (NAS)
negative regulation of canonical Wnt signaling pathway  (IMP)
negative regulation of cell motility  (IEA)
negative regulation of cell population proliferation  (IDA,IMP)
negative regulation of ERK1 and ERK2 cascade  (IDA)
negative regulation of fibroblast migration  (IEA,ISO)
negative regulation of mitotic cell cycle  (IMP)
negative regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction  (IEA,IMP,ISO,ISS)
negative regulation of platelet-derived growth factor receptor signaling pathway  (IEA,ISS)
negative regulation of sodium ion transport  (IEA,ISO)
nuclear migration  (IMP)
phospholipase C-activating dopamine receptor signaling pathway  (IEA,ISO)
plasma membrane organization  (IEA,ISS)
positive regulation of intrinsic apoptotic signaling pathway  (IDA)
positive regulation of monoatomic ion transmembrane transport  (IEA,ISO)
protein localization  (IEA,ISO)
protein localization to plasma membrane  (IBA,IEA,IMP)
protein-containing complex assembly  (TAS)
regulation of cell shape  (IMP)
regulation of cell size  (IMP)
regulation of renal phosphate excretion  (IEA,ISO)
renal absorption  (IEA,ISS)
renal phosphate ion absorption  (IMP)
renal sodium ion transport  (IEA,ISO)
sensory perception of sound  (IEA,ISO)
sodium ion transport  (IEA,ISO)
transport across blood-brain barrier  (NAS)
Wnt signaling pathway  (IEA)

Cellular Component

Molecular Pathway Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. Expression of the Na+/H+ exchanger regulatory protein family in genetically hypertensive rats. Kobayashi K, etal., J Hypertens. 2004 Sep;22(9):1723-30.
3. The parathyroid hormone receptorsome and the potential for therapeutic intervention. Mahon MJ Curr Drug Targets. 2012 Jan;13(1):116-28.
4. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
5. PID Annotation Import Pipeline Pipeline to import Pathway Interaction Database annotations from NCI into RGD
6. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
7. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
8. RGD HPO Phenotype Annotation Pipeline RGD automated import pipeline for human HPO-to-gene-to-disease annotations
Additional References at PubMed
PMID:7738182   PMID:9096337   PMID:9314537   PMID:9430655   PMID:9560162   PMID:9613608   PMID:9671706   PMID:9677412   PMID:10446210   PMID:10499588   PMID:10562288   PMID:10748165  
PMID:10852925   PMID:10980202   PMID:11046132   PMID:11099500   PMID:11158634   PMID:11285285   PMID:11304524   PMID:11352585   PMID:11526121   PMID:11533036   PMID:11684085   PMID:11882663  
PMID:11893083   PMID:11956211   PMID:11967229   PMID:12004055   PMID:12075354   PMID:12080081   PMID:12145337   PMID:12193606   PMID:12369822   PMID:12403779   PMID:12444018   PMID:12444019  
PMID:12471024   PMID:12477932   PMID:12499563   PMID:12615054   PMID:12621035   PMID:12626493   PMID:12651858   PMID:12665801   PMID:12830000   PMID:12881487   PMID:12920119   PMID:12954600  
PMID:14507927   PMID:14531806   PMID:14580213   PMID:14604981   PMID:14608357   PMID:14702039   PMID:14744877   PMID:15020681   PMID:15070904   PMID:15146197   PMID:15161943   PMID:15302935  
PMID:15342556   PMID:15467753   PMID:15489334   PMID:15523054   PMID:15553237   PMID:15805108   PMID:15932893   PMID:16129695   PMID:16236806   PMID:16456542   PMID:16519819   PMID:16615918  
PMID:17078868   PMID:17081983   PMID:17110338   PMID:17237149   PMID:17242191   PMID:17244609   PMID:17332506   PMID:17342744   PMID:17593079   PMID:17602283   PMID:17613530   PMID:17884816  
PMID:17895247   PMID:17911601   PMID:17982258   PMID:18029348   PMID:18045536   PMID:18184109   PMID:18407958   PMID:18559527   PMID:18588753   PMID:18754678   PMID:18784102   PMID:19027007  
PMID:19034380   PMID:19056867   PMID:19073137   PMID:19091402   PMID:19139211   PMID:19165527   PMID:19173579   PMID:19188335   PMID:19190083   PMID:19199708   PMID:19234136   PMID:19308292  
PMID:19446522   PMID:19555689   PMID:19581308   PMID:19591839   PMID:19615732   PMID:19912366   PMID:20012548   PMID:20031577   PMID:20042604   PMID:20140636   PMID:20203292   PMID:20237154  
PMID:20395446   PMID:20404332   PMID:20442317   PMID:20458337   PMID:20562104   PMID:20571032   PMID:20656684   PMID:20736378   PMID:20801883   PMID:20802536   PMID:20937695   PMID:21160026  
PMID:21170265   PMID:21191106   PMID:21203899   PMID:21496870   PMID:21672215   PMID:21680517   PMID:21707710   PMID:21804599   PMID:21822312   PMID:21832055   PMID:21873635   PMID:21971156  
PMID:21983488   PMID:21988832   PMID:21990315   PMID:22028271   PMID:22190034   PMID:22354994   PMID:22366766   PMID:22440733   PMID:22446018   PMID:22466651   PMID:22476347   PMID:22496422  
PMID:22506049   PMID:22610101   PMID:22622406   PMID:22628548   PMID:22766563   PMID:22801783   PMID:22855531   PMID:22863883   PMID:22939629   PMID:22964850   PMID:23118026   PMID:23284683  
PMID:23376485   PMID:23397142   PMID:23414517   PMID:23454118   PMID:23483729   PMID:23533145   PMID:23583913   PMID:23775624   PMID:23985317   PMID:24012959   PMID:24201803   PMID:24339979  
PMID:24642259   PMID:24728453   PMID:24768637   PMID:24788249   PMID:24862762   PMID:25163515   PMID:25468996   PMID:25492869   PMID:25555876   PMID:25744438   PMID:25756512   PMID:25775275  
PMID:25789870   PMID:25921289   PMID:25990958   PMID:26045165   PMID:26126066   PMID:26142394   PMID:26218645   PMID:26344197   PMID:26432781   PMID:26491017   PMID:26496610   PMID:26531778  
PMID:26618866   PMID:26641092   PMID:26789121   PMID:26862730   PMID:26977012   PMID:27097111   PMID:27107012   PMID:27173435   PMID:27206858   PMID:27448983   PMID:27509846   PMID:27566107  
PMID:27576135   PMID:27684187   PMID:27765918   PMID:27793802   PMID:27823775   PMID:27871951   PMID:27880917   PMID:27999191   PMID:28011475   PMID:28068322   PMID:28085111   PMID:28235801  
PMID:28285124   PMID:28360110   PMID:28376304   PMID:28388416   PMID:28392297   PMID:28514442   PMID:28535016   PMID:28684865   PMID:28739728   PMID:28739734   PMID:28960081   PMID:29126251  
PMID:29551770   PMID:29568061   PMID:29846905   PMID:29867145   PMID:29901158   PMID:30230542   PMID:30280653   PMID:30575818   PMID:30581004   PMID:30631154   PMID:30696771   PMID:30833792  
PMID:31042404   PMID:31171716   PMID:31324722   PMID:31932471   PMID:32014995   PMID:32164629   PMID:32296183   PMID:32513696   PMID:32801337   PMID:32994395   PMID:33092043   PMID:33499384  
PMID:33639163   PMID:33864728   PMID:33952618   PMID:33961781   PMID:33965858   PMID:34079125   PMID:34189428   PMID:34323956   PMID:34709727   PMID:34835087   PMID:35140182   PMID:35256949  
PMID:35271311   PMID:35307350   PMID:35384245   PMID:35819319   PMID:35831314   PMID:35944360   PMID:36012204   PMID:36215168   PMID:36225252   PMID:36762943   PMID:37232246   PMID:37689310  
PMID:38117590  


Genomics

Comparative Map Data
NHERF1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381774,748,628 - 74,769,353 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1774,748,628 - 74,769,353 (+)EnsemblGRCh38hg38GRCh38
GRCh371772,744,767 - 72,765,492 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361770,256,373 - 70,277,089 (+)NCBINCBI36Build 36hg18NCBI36
Build 341770,256,378 - 70,277,089NCBI
Celera1769,337,944 - 69,358,679 (+)NCBICelera
Cytogenetic Map17q25.1NCBI
HuRef1768,155,124 - 68,175,866 (+)NCBIHuRef
CHM1_11772,809,571 - 72,830,338 (+)NCBICHM1_1
T2T-CHM13v2.01775,640,506 - 75,661,228 (+)NCBIT2T-CHM13v2.0
Nherf1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm3911115,054,138 - 115,072,009 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl11115,054,167 - 115,072,007 (+)EnsemblGRCm39 Ensembl
GRCm3811115,163,341 - 115,181,178 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl11115,163,341 - 115,181,181 (+)EnsemblGRCm38mm10GRCm38
MGSCv3711115,024,655 - 115,042,492 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv3611114,979,493 - 115,014,684 (+)NCBIMGSCv36mm8
Celera11126,928,560 - 126,946,416 (+)NCBICelera
Cytogenetic Map11E2NCBI
cM Map1180.65NCBI
Nherf1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr810100,902,165 - 100,919,265 (+)NCBIGRCr8
mRatBN7.210100,403,189 - 100,420,290 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl10100,403,069 - 100,420,598 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx10105,463,056 - 105,480,181 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.010104,926,121 - 104,943,248 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.010100,324,177 - 100,341,277 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.010103,713,045 - 103,730,145 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl10103,713,045 - 103,730,145 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.010104,573,624 - 104,590,426 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.410105,237,637 - 105,254,750 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.110105,252,140 - 105,269,254 (+)NCBI
Celera1098,979,637 - 98,995,900 (+)NCBICelera
Cytogenetic Map10q32.1NCBI
Nherf1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049555531,639,267 - 1,656,850 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049555531,639,267 - 1,656,850 (+)NCBIChiLan1.0ChiLan1.0
NHERF1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21990,785,997 - 90,806,905 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11795,608,707 - 95,629,599 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01768,694,468 - 68,715,157 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11774,250,406 - 74,271,234 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1774,250,406 - 74,271,234 (+)Ensemblpanpan1.1panPan2
NHERF1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.195,661,792 - 5,679,783 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl95,662,464 - 5,679,570 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha96,341,827 - 6,358,910 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.096,333,687 - 6,351,685 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl96,333,688 - 6,351,686 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.196,371,237 - 6,388,311 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.096,481,877 - 6,498,929 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.096,542,206 - 6,559,311 (-)NCBIUU_Cfam_GSD_1.0
Nherf1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_0244056026,275,339 - 6,292,156 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_004936594119,770 - 136,789 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_004936594119,808 - 136,620 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
NHERF1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl126,466,121 - 6,483,548 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1126,466,138 - 6,483,539 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2126,455,107 - 6,472,510 (-)NCBISscrofa10.2Sscrofa10.2susScr3
NHERF1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11646,889,454 - 46,910,776 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1646,888,942 - 46,910,842 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366607717,675,824 - 17,696,157 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Nherf1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248014,612,849 - 4,630,451 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248014,612,890 - 4,630,454 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in NHERF1
119 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_004252.5(NHERF1):c.203A>C (p.Glu68Ala) single nucleotide variant not provided [RCV000521667] Chr17:74749049 [GRCh38]
Chr17:72745188 [GRCh37]
Chr17:17q25.1		 conflicting interpretations of pathogenicity|uncertain significance
NM_004252.5(NHERF1):c.328C>G (p.Leu110Val) single nucleotide variant Hypophosphatemic nephrolithiasis/osteoporosis 2 [RCV000005588]|not provided [RCV001514734]|not specified [RCV001701718] Chr17:74749174 [GRCh38]
Chr17:72745313 [GRCh37]
Chr17:17q25.1		 pathogenic|benign|conflicting interpretations of pathogenicity|uncertain significance
NM_004252.5(NHERF1):c.458G>A (p.Arg153Gln) single nucleotide variant Chronic kidney disease [RCV001171340]|Hypophosphatemic nephrolithiasis/osteoporosis 2 [RCV000005589]|NHERF1-related condition [RCV003914809]|not provided [RCV000484640] Chr17:74762028 [GRCh38]
Chr17:72758167 [GRCh37]
Chr17:17q25.1		 pathogenic|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_004252.5(NHERF1):c.673G>A (p.Glu225Lys) single nucleotide variant Hypophosphatemic nephrolithiasis/osteoporosis 2 [RCV000005590]|NHERF1-related condition [RCV003914810]|Nephrolithiasis [RCV000662330]|not provided [RCV002054417]|not specified [RCV000454997] Chr17:74763436 [GRCh38]
Chr17:72759575 [GRCh37]
Chr17:17q25.1		 pathogenic|likely pathogenic|benign|likely benign
GRCh38/hg38 17q24.3-25.3(chr17:69209079-83086677)x3 copy number gain See cases [RCV000052486] Chr17:69209079..83086677 [GRCh38]
Chr17:67205220..81044553 [GRCh37]
Chr17:64716815..78637842 [NCBI36]
Chr17:17q24.3-25.3		 pathogenic
GRCh38/hg38 17q23.2-25.3(chr17:36449220-83086677)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]|See cases [RCV000052483] Chr17:36449220..83086677 [GRCh38]
Chr17:58617905..81044553 [GRCh37]
Chr17:55972687..78637842 [NCBI36]
Chr17:17q23.2-25.3		 pathogenic
NM_004252.5(NHERF1):c.1030C>G (p.Pro344Ala) single nucleotide variant not provided [RCV000054711] Chr17:74768609 [GRCh38]
Chr17:72764748 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.33G>T (p.Leu11=) single nucleotide variant not provided [RCV000054712] Chr17:74748879 [GRCh38]
Chr17:72745018 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.708C>G (p.Asp236Glu) single nucleotide variant not provided [RCV000054713] Chr17:74763471 [GRCh38]
Chr17:72759610 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.958A>T (p.Ile320Phe) single nucleotide variant not provided [RCV000054714] Chr17:74768537 [GRCh38]
Chr17:72764676 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.202_204del (p.Glu68del) deletion not provided [RCV000722205] Chr17:74749047..74749049 [GRCh38]
Chr17:72745186..72745188 [GRCh37]
Chr17:17q25.1		 uncertain significance
GRCh38/hg38 17q23.1-25.1(chr17:36449220-75053130)x3 copy number gain See cases [RCV000137437] Chr17:36449220..75053130 [GRCh38]
Chr17:57595736..73049225 [GRCh37]
Chr17:54950518..70560820 [NCBI36]
Chr17:17q23.1-25.1		 pathogenic
GRCh38/hg38 17q24.3-25.3(chr17:69916435-83102552)x3 copy number gain See cases [RCV000143342] Chr17:69916435..83102552 [GRCh38]
Chr17:67912576..81048189 [GRCh37]
Chr17:65424171..78653717 [NCBI36]
Chr17:17q24.3-25.3		 pathogenic
GRCh37/hg19 17q24.2-25.3(chr17:64241326-81041938)x3 copy number gain See cases [RCV000447577] Chr17:64241326..81041938 [GRCh37]
Chr17:17q24.2-25.3		 pathogenic
GRCh37/hg19 17q21.31-25.3(chr17:42580684-81085615)x3 copy number gain See cases [RCV000447823] Chr17:42580684..81085615 [GRCh37]
Chr17:17q21.31-25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938) copy number gain See cases [RCV000511439] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17q25.1(chr17:72718277-74142256) copy number gain 7q11.23 microduplication syndrome [RCV003325440] Chr17:72718277..74142256 [GRCh37]
Chr17:17q25.1		 pathogenic
NM_004252.5(NHERF1):c.307G>T (p.Gly103Cys) single nucleotide variant Inborn genetic diseases [RCV003243934]|not provided [RCV003730480] Chr17:74749153 [GRCh38]
Chr17:72745292 [GRCh37]
Chr17:17q25.1		 uncertain significance
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3 copy number gain See cases [RCV000512441] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17q24.2-25.3(chr17:67002415-81041938)x3 copy number gain See cases [RCV000512573] Chr17:67002415..81041938 [GRCh37]
Chr17:17q24.2-25.3		 pathogenic
NM_004252.5(NHERF1):c.657C>G (p.Ile219Met) single nucleotide variant Hypophosphatemic nephrolithiasis/osteoporosis 2 [RCV000680101]|NHERF1-related condition [RCV003965432]|not provided [RCV001065657] Chr17:74763420 [GRCh38]
Chr17:72759559 [GRCh37]
Chr17:17q25.1		 likely benign|uncertain significance
GRCh37/hg19 17q24.1-25.3(chr17:63689671-81041938)x3 copy number gain not provided [RCV000683952] Chr17:63689671..81041938 [GRCh37]
Chr17:17q24.1-25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:8547-81060040)x3 copy number gain not provided [RCV000739324] Chr17:8547..81060040 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:7214-81058310)x3 copy number gain not provided [RCV000739320] Chr17:7214..81058310 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:12344-81057996)x3 copy number gain not provided [RCV000739325] Chr17:12344..81057996 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
NC_000017.11:g.74748373T>C single nucleotide variant not provided [RCV001667972] Chr17:74748373 [GRCh38]
Chr17:72744512 [GRCh37]
Chr17:17q25.1		 benign
GRCh37/hg19 17q24.1-25.2(chr17:64159738-74891024)x3 copy number gain not provided [RCV000762750] Chr17:64159738..74891024 [GRCh37]
Chr17:17q24.1-25.2		 likely pathogenic
NM_004252.5(NHERF1):c.-116C>T single nucleotide variant not provided [RCV003315073] Chr17:74748731 [GRCh38]
Chr17:72744870 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.799-177A>G single nucleotide variant not provided [RCV001709940] Chr17:74767970 [GRCh38]
Chr17:72764109 [GRCh37]
Chr17:17q25.1		 benign
NM_004252.5(NHERF1):c.267G>A (p.Leu89=) single nucleotide variant NHERF1-related condition [RCV003930490]|not provided [RCV000879882] Chr17:74749113 [GRCh38]
Chr17:72745252 [GRCh37]
Chr17:17q25.1		 benign
NM_004252.5(NHERF1):c.132C>T (p.Pro44=) single nucleotide variant NHERF1-related condition [RCV003930854]|not provided [RCV000893866] Chr17:74748978 [GRCh38]
Chr17:72745117 [GRCh37]
Chr17:17q25.1		 benign
NM_004252.5(NHERF1):c.627G>A (p.Gly209=) single nucleotide variant not provided [RCV000906250] Chr17:74763390 [GRCh38]
Chr17:72759529 [GRCh37]
Chr17:17q25.1		 benign|likely benign
GRCh37/hg19 17q24.3-25.1(chr17:70720436-73175266) copy number gain not provided [RCV000767767] Chr17:70720436..73175266 [GRCh37]
Chr17:17q24.3-25.1		 pathogenic
GRCh37/hg19 17q24.1-25.3(chr17:62778720-81041938)x3 copy number gain not provided [RCV000849900] Chr17:62778720..81041938 [GRCh37]
Chr17:17q24.1-25.3		 pathogenic
NM_004252.5(NHERF1):c.-188G>C single nucleotide variant not provided [RCV001692742] Chr17:74748659 [GRCh38]
Chr17:72744798 [GRCh37]
Chr17:17q25.1		 benign
NC_000017.11:g.74748444A>C single nucleotide variant not provided [RCV001656419] Chr17:74748444 [GRCh38]
Chr17:72744583 [GRCh37]
Chr17:17q25.1		 benign
NM_004252.5(NHERF1):c.518C>T (p.Ser173Phe) single nucleotide variant NHERF1-related condition [RCV003930698]|not provided [RCV000887508] Chr17:74762088 [GRCh38]
Chr17:72758227 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.758-174A>T single nucleotide variant not provided [RCV001688224] Chr17:74766762 [GRCh38]
Chr17:72762901 [GRCh37]
Chr17:17q25.1		 benign
NM_004252.5(NHERF1):c.758-192C>T single nucleotide variant not provided [RCV001694309] Chr17:74766744 [GRCh38]
Chr17:72762883 [GRCh37]
Chr17:17q25.1		 benign
NM_004252.5(NHERF1):c.758-322A>G single nucleotide variant not provided [RCV001724703] Chr17:74766614 [GRCh38]
Chr17:72762753 [GRCh37]
Chr17:17q25.1		 benign
NM_004252.5(NHERF1):c.888+2T>C single nucleotide variant not provided [RCV001035882] Chr17:74768238 [GRCh38]
Chr17:72764377 [GRCh37]
Chr17:17q25.1		 conflicting interpretations of pathogenicity|uncertain significance
NM_004252.5(NHERF1):c.469A>C (p.Met157Leu) single nucleotide variant Hypophosphatemic nephrolithiasis/osteoporosis 2 [RCV002491750]|not provided [RCV001233214] Chr17:74762039 [GRCh38]
Chr17:72758178 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.1057G>C (p.Glu353Gln) single nucleotide variant not provided [RCV001318608] Chr17:74768636 [GRCh38]
Chr17:72764775 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.581G>A (p.Arg194Gln) single nucleotide variant Inborn genetic diseases [RCV003284262]|not provided [RCV001361700] Chr17:74762151 [GRCh38]
Chr17:72758290 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.248T>G (p.Leu83Arg) single nucleotide variant not provided [RCV001349782] Chr17:74749094 [GRCh38]
Chr17:72745233 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.425A>G (p.Lys142Arg) single nucleotide variant Hypophosphatemic nephrolithiasis/osteoporosis 2 [RCV002486138]|not provided [RCV001297572] Chr17:74749271 [GRCh38]
Chr17:72745410 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.709G>A (p.Glu237Lys) single nucleotide variant not provided [RCV001318918] Chr17:74763472 [GRCh38]
Chr17:72759611 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.89G>A (p.Gly30Glu) single nucleotide variant not provided [RCV001354381] Chr17:74748935 [GRCh38]
Chr17:72745074 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.501C>T (p.Asn167=) single nucleotide variant not provided [RCV001515806] Chr17:74762071 [GRCh38]
Chr17:72758210 [GRCh37]
Chr17:17q25.1		 benign
NM_004252.5(NHERF1):c.902A>T (p.Asp301Val) single nucleotide variant NHERF1-related condition [RCV003973248]|not provided [RCV001411748] Chr17:74768481 [GRCh38]
Chr17:72764620 [GRCh37]
Chr17:17q25.1		 benign|likely benign
NM_004252.5(NHERF1):c.441+14A>G single nucleotide variant not provided [RCV001518768] Chr17:74749301 [GRCh38]
Chr17:72745440 [GRCh37]
Chr17:17q25.1		 benign
NM_004252.5(NHERF1):c.555C>A (p.Asp185Glu) single nucleotide variant not provided [RCV001512437] Chr17:74762125 [GRCh38]
Chr17:72758264 [GRCh37]
Chr17:17q25.1		 benign|likely benign
NM_004252.5(NHERF1):c.432C>T (p.His144=) single nucleotide variant not provided [RCV001727052] Chr17:74749278 [GRCh38]
Chr17:72745417 [GRCh37]
Chr17:17q25.1		 benign|likely benign
NC_000017.11:g.74748473G>A single nucleotide variant not provided [RCV001774833] Chr17:74748473 [GRCh38]
Chr17:72744612 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.-43C>A single nucleotide variant not provided [RCV001757570] Chr17:74748804 [GRCh38]
Chr17:72744943 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.-75G>A single nucleotide variant not provided [RCV001757287] Chr17:74748772 [GRCh38]
Chr17:72744911 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.406G>T (p.Glu136Ter) single nucleotide variant not provided [RCV001968922] Chr17:74749252 [GRCh38]
Chr17:72745391 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.539G>T (p.Arg180Leu) single nucleotide variant not provided [RCV001955724] Chr17:74762109 [GRCh38]
Chr17:72758248 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.445G>A (p.Glu149Lys) single nucleotide variant not provided [RCV001934379] Chr17:74762015 [GRCh38]
Chr17:72758154 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.940A>G (p.Thr314Ala) single nucleotide variant Hypophosphatemic nephrolithiasis/osteoporosis 2 [RCV002507649]|not provided [RCV001978688] Chr17:74768519 [GRCh38]
Chr17:72764658 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.325G>T (p.Glu109Ter) single nucleotide variant not provided [RCV001959404] Chr17:74749171 [GRCh38]
Chr17:72745310 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.44G>T (p.Cys15Phe) single nucleotide variant not provided [RCV002049103] Chr17:74748890 [GRCh38]
Chr17:72745029 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.913A>G (p.Lys305Glu) single nucleotide variant Hypophosphatemic nephrolithiasis/osteoporosis 2 [RCV002486582]|not provided [RCV001989495] Chr17:74768492 [GRCh38]
Chr17:72764631 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.252C>T (p.Asn84=) single nucleotide variant Hypophosphatemic nephrolithiasis/osteoporosis 2 [RCV002494449]|not provided [RCV002145705] Chr17:74749098 [GRCh38]
Chr17:72745237 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.538C>T (p.Arg180Trp) single nucleotide variant not provided [RCV002072453] Chr17:74762108 [GRCh38]
Chr17:72758247 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.888+13T>C single nucleotide variant Hypophosphatemic nephrolithiasis/osteoporosis 2 [RCV002498227]|not provided [RCV002212882] Chr17:74768249 [GRCh38]
Chr17:72764388 [GRCh37]
Chr17:17q25.1		 benign|likely benign
NM_004252.5(NHERF1):c.85C>A (p.His29Asn) single nucleotide variant Hypophosphatemic nephrolithiasis/osteoporosis 2 [RCV002500343]|not provided [RCV002173965] Chr17:74748931 [GRCh38]
Chr17:72745070 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.804C>T (p.Asn268=) single nucleotide variant not provided [RCV002137922] Chr17:74768152 [GRCh38]
Chr17:72764291 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.130C>G (p.Pro44Ala) single nucleotide variant not provided [RCV002140435] Chr17:74748976 [GRCh38]
Chr17:72745115 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.1000G>A (p.Ala334Thr) single nucleotide variant not provided [RCV002304604] Chr17:74768579 [GRCh38]
Chr17:72764718 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.286G>A (p.Asp96Asn) single nucleotide variant Inborn genetic diseases [RCV003201918] Chr17:74749132 [GRCh38]
Chr17:72745271 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.560C>T (p.Pro187Leu) single nucleotide variant Inborn genetic diseases [RCV003371421]|not provided [RCV003778048] Chr17:74762130 [GRCh38]
Chr17:72758269 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.71A>G (p.Tyr24Cys) single nucleotide variant not provided [RCV003421472] Chr17:74748917 [GRCh38]
Chr17:72745056 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.154G>A (p.Gly52Arg) single nucleotide variant Inborn genetic diseases [RCV003351112] Chr17:74749000 [GRCh38]
Chr17:72745139 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.910C>G (p.Pro304Ala) single nucleotide variant not provided [RCV003543871] Chr17:74768489 [GRCh38]
Chr17:72764628 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.1056C>T (p.Asn352=) single nucleotide variant not provided [RCV003570740] Chr17:74768635 [GRCh38]
Chr17:72764774 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.458G>T (p.Arg153Leu) single nucleotide variant not provided [RCV003571005] Chr17:74762028 [GRCh38]
Chr17:72758167 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.603+17T>G single nucleotide variant not provided [RCV003569072] Chr17:74762190 [GRCh38]
Chr17:72758329 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.319C>G (p.Arg107Gly) single nucleotide variant NHERF1-related condition [RCV003404430] Chr17:74749165 [GRCh38]
Chr17:72745304 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.391G>C (p.Ala131Pro) single nucleotide variant not provided [RCV003428463] Chr17:74749237 [GRCh38]
Chr17:72745376 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.26C>A (p.Ala9Glu) single nucleotide variant NHERF1-related condition [RCV003412376] Chr17:74748872 [GRCh38]
Chr17:72745011 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.261C>T (p.Arg87=) single nucleotide variant not provided [RCV003413332] Chr17:74749107 [GRCh38]
Chr17:72745246 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.260G>T (p.Arg87Leu) single nucleotide variant not provided [RCV003428461] Chr17:74749106 [GRCh38]
Chr17:72745245 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.758-3T>C single nucleotide variant not provided [RCV003428464] Chr17:74766933 [GRCh38]
Chr17:72763072 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.366G>C (p.Pro122=) single nucleotide variant not provided [RCV003428462] Chr17:74749212 [GRCh38]
Chr17:72745351 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.718A>C (p.Lys240Gln) single nucleotide variant not provided [RCV003421473] Chr17:74763481 [GRCh38]
Chr17:72759620 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.1031C>T (p.Pro344Leu) single nucleotide variant not provided [RCV003421474] Chr17:74768610 [GRCh38]
Chr17:72764749 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.757+18A>G single nucleotide variant not provided [RCV003879755] Chr17:74763538 [GRCh38]
Chr17:72759677 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.122T>A (p.Leu41Gln) single nucleotide variant not provided [RCV003826530] Chr17:74748968 [GRCh38]
Chr17:72745107 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.693G>A (p.Val231=) single nucleotide variant not provided [RCV003547892] Chr17:74763456 [GRCh38]
Chr17:72759595 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.326A>T (p.Glu109Val) single nucleotide variant not provided [RCV003876042] Chr17:74749172 [GRCh38]
Chr17:72745311 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.521A>G (p.Lys174Arg) single nucleotide variant not provided [RCV003739902] Chr17:74762091 [GRCh38]
Chr17:72758230 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.137C>T (p.Ser46Leu) single nucleotide variant not provided [RCV003829135] Chr17:74748983 [GRCh38]
Chr17:72745122 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.809G>A (p.Arg270His) single nucleotide variant Hypophosphatemic nephrolithiasis/osteoporosis 2 [RCV003984376]|not provided [RCV003544617] Chr17:74768157 [GRCh38]
Chr17:72764296 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.888+18G>C single nucleotide variant not provided [RCV003824778] Chr17:74768254 [GRCh38]
Chr17:72764393 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.708C>T (p.Asp236=) single nucleotide variant not provided [RCV003693143] Chr17:74763471 [GRCh38]
Chr17:72759610 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.603+4A>G single nucleotide variant not provided [RCV003715304] Chr17:74762177 [GRCh38]
Chr17:72758316 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.561G>C (p.Pro187=) single nucleotide variant not provided [RCV003546026] Chr17:74762131 [GRCh38]
Chr17:72758270 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.604-6C>T single nucleotide variant not provided [RCV003546095] Chr17:74763361 [GRCh38]
Chr17:72759500 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.659G>A (p.Arg220Lys) single nucleotide variant not provided [RCV003545558] Chr17:74763422 [GRCh38]
Chr17:72759561 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.463T>C (p.Cys155Arg) single nucleotide variant not provided [RCV003717158] Chr17:74762033 [GRCh38]
Chr17:72758172 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.120G>T (p.Arg40=) single nucleotide variant not provided [RCV003699124] Chr17:74748966 [GRCh38]
Chr17:72745105 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.165G>C (p.Ala55=) single nucleotide variant not provided [RCV003717087] Chr17:74749011 [GRCh38]
Chr17:72745150 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.441+13_441+14inv inversion not provided [RCV003856106] Chr17:74749300..74749301 [GRCh38]
Chr17:72745439..72745440 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.1032G>A (p.Pro344=) single nucleotide variant not provided [RCV003837228] Chr17:74768611 [GRCh38]
Chr17:72764750 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.808C>T (p.Arg270Cys) single nucleotide variant not provided [RCV003726477] Chr17:74768156 [GRCh38]
Chr17:72764295 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.744G>A (p.Gln248=) single nucleotide variant not provided [RCV003855862] Chr17:74763507 [GRCh38]
Chr17:72759646 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.978C>T (p.Ser326=) single nucleotide variant not provided [RCV003667549] Chr17:74768557 [GRCh38]
Chr17:72764696 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.667G>A (p.Gly223Arg) single nucleotide variant not provided [RCV003724400] Chr17:74763430 [GRCh38]
Chr17:72759569 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.966C>A (p.Asp322Glu) single nucleotide variant not provided [RCV003835744] Chr17:74768545 [GRCh38]
Chr17:72764684 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.611G>T (p.Gly204Val) single nucleotide variant not provided [RCV003669776] Chr17:74763374 [GRCh38]
Chr17:72759513 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.1008G>A (p.Gln336=) single nucleotide variant not provided [RCV003814399] Chr17:74768587 [GRCh38]
Chr17:72764726 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.539G>A (p.Arg180Gln) single nucleotide variant NHERF1-related condition [RCV003919327]|not provided [RCV003724237] Chr17:74762109 [GRCh38]
Chr17:72758248 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.917A>G (p.Gln306Arg) single nucleotide variant not provided [RCV003668037] Chr17:74768496 [GRCh38]
Chr17:72764635 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.150G>A (p.Lys50=) single nucleotide variant not provided [RCV003579654] Chr17:74748996 [GRCh38]
Chr17:72745135 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.426G>C (p.Lys142Asn) single nucleotide variant not provided [RCV003717088] Chr17:74749272 [GRCh38]
Chr17:72745411 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.255C>T (p.Ala85=) single nucleotide variant not provided [RCV003672720] Chr17:74749101 [GRCh38]
Chr17:72745240 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.259dup (p.Arg87fs) duplication not provided [RCV003666676] Chr17:74749104..74749105 [GRCh38]
Chr17:72745243..72745244 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.5G>A (p.Ser2Asn) single nucleotide variant not provided [RCV003566416] Chr17:74748851 [GRCh38]
Chr17:72744990 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.457C>T (p.Arg153Trp) single nucleotide variant not provided [RCV003866590] Chr17:74762027 [GRCh38]
Chr17:72758166 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.805A>G (p.Ser269Gly) single nucleotide variant not provided [RCV003562602] Chr17:74768153 [GRCh38]
Chr17:72764292 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.441+8G>A single nucleotide variant not provided [RCV003705796] Chr17:74749295 [GRCh38]
Chr17:72745434 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.102G>C (p.Lys34Asn) single nucleotide variant not provided [RCV003730008] Chr17:74748948 [GRCh38]
Chr17:72745087 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.325_326delinsTT (p.Glu109Leu) indel not provided [RCV003732850] Chr17:74749171..74749172 [GRCh38]
Chr17:72745310..72745311 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.839G>A (p.Ser280Asn) single nucleotide variant not provided [RCV003542215] Chr17:74768187 [GRCh38]
Chr17:72764326 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.936G>A (p.Ser312=) single nucleotide variant not provided [RCV003555307] Chr17:74768515 [GRCh38]
Chr17:72764654 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.943T>A (p.Ser315Thr) single nucleotide variant not provided [RCV003731022] Chr17:74768522 [GRCh38]
Chr17:72764661 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.359C>T (p.Ala120Val) single nucleotide variant not provided [RCV003822415] Chr17:74749205 [GRCh38]
Chr17:72745344 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.466A>G (p.Thr156Ala) single nucleotide variant not provided [RCV003853445] Chr17:74762036 [GRCh38]
Chr17:72758175 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.791T>C (p.Ile264Thr) single nucleotide variant not provided [RCV003674800] Chr17:74766969 [GRCh38]
Chr17:72763108 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.758-14T>G single nucleotide variant not provided [RCV003678047] Chr17:74766922 [GRCh38]
Chr17:72763061 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.491A>T (p.Tyr164Phe) single nucleotide variant not provided [RCV003865526] Chr17:74762061 [GRCh38]
Chr17:72758200 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.330G>C (p.Leu110=) single nucleotide variant not provided [RCV003737377] Chr17:74749176 [GRCh38]
Chr17:72745315 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.888+21dup duplication not provided [RCV003865308] Chr17:74768251..74768252 [GRCh38]
Chr17:72764390..72764391 [GRCh37]
Chr17:17q25.1		 benign
NM_004252.5(NHERF1):c.337G>C (p.Ala113Pro) single nucleotide variant not provided [RCV003732143] Chr17:74749183 [GRCh38]
Chr17:72745322 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.210G>A (p.Glu70=) single nucleotide variant not provided [RCV003552963] Chr17:74749056 [GRCh38]
Chr17:72745195 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.420C>G (p.Ala140=) single nucleotide variant not provided [RCV003712227] Chr17:74749266 [GRCh38]
Chr17:72745405 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.8C>T (p.Ala3Val) single nucleotide variant not provided [RCV003818422] Chr17:74748854 [GRCh38]
Chr17:72744993 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.757+13G>A single nucleotide variant not provided [RCV003705428] Chr17:74763533 [GRCh38]
Chr17:72759672 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.242C>T (p.Ala81Val) single nucleotide variant not provided [RCV003553589] Chr17:74749088 [GRCh38]
Chr17:72745227 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.609C>T (p.Asn203=) single nucleotide variant not provided [RCV003887515] Chr17:74763372 [GRCh38]
Chr17:72759511 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.855G>A (p.Leu285=) single nucleotide variant NHERF1-related condition [RCV003967408] Chr17:74768203 [GRCh38]
Chr17:72764342 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.107G>A (p.Gly36Asp) single nucleotide variant Hypophosphatemic nephrolithiasis/osteoporosis 2 [RCV003984464] Chr17:74748953 [GRCh38]
Chr17:72745092 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_004252.5(NHERF1):c.672C>T (p.Asp224=) single nucleotide variant NHERF1-related condition [RCV003979131] Chr17:74763435 [GRCh38]
Chr17:72759574 [GRCh37]
Chr17:17q25.1		 likely benign
NM_004252.5(NHERF1):c.441+7G>A single nucleotide variant NHERF1-related condition [RCV003932050] Chr17:74749294 [GRCh38]
Chr17:72745433 [GRCh37]
Chr17:17q25.1		 benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1836
Count of miRNA genes:630
Interacting mature miRNAs:713
Transcripts:ENST00000262613, ENST00000413388, ENST00000578958, ENST00000581356, ENST00000583369
Prediction methods:Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region
RH92683  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371772,743,304 - 72,743,428UniSTSGRCh37
Build 361770,254,899 - 70,255,023RGDNCBI36
Celera1769,336,485 - 69,336,609RGD
Cytogenetic Map17q25.1UniSTS
HuRef1768,153,677 - 68,153,801UniSTS
GeneMap99-GB4 RH Map17471.85UniSTS
RH98250  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371772,765,210 - 72,765,363UniSTSGRCh37
Build 361770,276,805 - 70,276,958RGDNCBI36
Celera1769,358,390 - 69,358,543RGD
Cytogenetic Map17q25.1UniSTS
GeneMap99-GB4 RH Map17472.92UniSTS
G19962  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371772,765,278 - 72,765,377UniSTSGRCh37
Build 361770,276,873 - 70,276,972RGDNCBI36
Celera1769,358,458 - 69,358,557RGD
Cytogenetic Map17q25.1UniSTS
HuRef1768,175,645 - 68,175,744UniSTS
A002D35  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371772,765,278 - 72,765,377UniSTSGRCh37
Build 361770,276,873 - 70,276,972RGDNCBI36
Celera1769,358,458 - 69,358,557RGD
Cytogenetic Map17q25.1UniSTS
HuRef1768,175,645 - 68,175,744UniSTS
GeneMap99-GB4 RH Map17473.47UniSTS
NCBI RH Map17756.2UniSTS
SLC9A3R1_7238  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371772,764,874 - 72,765,563UniSTSGRCh37
Build 361770,276,469 - 70,277,158RGDNCBI36
Celera1769,358,054 - 69,358,743RGD
HuRef1768,175,241 - 68,175,930UniSTS
HUM000S150  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371772,765,302 - 72,765,478UniSTSGRCh37
Build 361770,276,897 - 70,277,073RGDNCBI36
Celera1769,358,482 - 69,358,658RGD
Cytogenetic Map17q25.1UniSTS
HuRef1768,175,669 - 68,175,845UniSTS
Stanford-G3 RH Map173221.0UniSTS
NCBI RH Map17767.8UniSTS
GeneMap99-G3 RH Map173722.0UniSTS
D10S16   No map positions available.
G35510  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map1q21UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map2p25-p24UniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map4q21.3UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map1p35UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map6pter-q22.33UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map11q14.2-q21UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map9p21.3UniSTS
Cytogenetic Map7p15.1UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map5q31-q32UniSTS
Cytogenetic Map18p11.2UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map12p13.33UniSTS
Cytogenetic Map18p11.22-p11.21UniSTS
Cytogenetic Map5q34-q35UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map7p14.2UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map11q13.3UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic Map12q13.1-q13.2UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic MapXp22.32UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map6pter-p12.1UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map17pUniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map20q13.33UniSTS
D10S275  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map13q12.13UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map14q22-q24UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map10p11UniSTS
Cytogenetic Map1p13.1UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map6q24UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map3p25UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map9q22UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic MapXp22.2-p22.1UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map20pter-q11.23UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map10p12.3UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map3q26.3UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map1q24-q25.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map12q24.32UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map11p14.3UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map4q13UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map7p14.2UniSTS
Cytogenetic Map6q24.3UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map6q12-q13UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map2p14UniSTS
RH36905  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map12q24.11UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map18p11.3-p11.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map3q27-q28UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map3q26.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map3q12.2-q12.3UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q12-q13.1UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map18p11.2UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map9q31.1UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map10q21UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map4q25-q27UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map10q24.1UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map10q25-q26UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map16q22.1UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map5q32-q34UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map8p22-p21UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map20q13.33UniSTS
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Cytogenetic Map7q36.2UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q33-q34UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map13q32UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map3p26.3UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic MapXp21.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3q24UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map14q11.2-q12UniSTS
Cytogenetic Map3p24UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS
D10S16  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map2q11.2-q12UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map3p22UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map9p13.3-p12UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map5q21-q22UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map1q24.1UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map4q34UniSTS
Cytogenetic Map2p22-p21UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map1p36.23UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map11p15.3-p15.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map3q26UniSTS
Cytogenetic Map12p12.1-p11.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic MapXq23UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map5p15.1UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map17qterUniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map20q12-q13.12UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map1pter-q31.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map3p23-p21UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1p36.1-p34UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.1-q21.2UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map13q12UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic MapXq21UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map15q24.2UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map2q34UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map3p23UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic Map4p15.3UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map9p22.3UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map19qterUniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map17pUniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map2p13.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map3q26.2UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High 1 1 1 4 1
Medium 2143 2454 1720 622 1943 463 3535 1052 3718 416 1440 1608 175 1 1202 1972 6 2
Low 296 537 5 1 7 1 822 1144 16 3 16 4 2 816
Below cutoff

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_013022 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_004252 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002958087 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC016888 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF015926 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF036241 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI203594 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK026581 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK094467 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK128474 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK312498 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC001443 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC003361 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC011777 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC049220 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC053350 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BP347679 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX648303 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471099 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CN286501 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068261 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CX761192 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000262613   ⟹   ENSP00000262613
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1774,748,628 - 74,769,353 (+)Ensembl
RefSeq Acc Id: ENST00000413388   ⟹   ENSP00000464982
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1774,762,003 - 74,769,296 (+)Ensembl
RefSeq Acc Id: ENST00000578958
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1774,763,030 - 74,768,559 (+)Ensembl
RefSeq Acc Id: ENST00000581356   ⟹   ENSP00000464117
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1774,763,428 - 74,768,803 (+)Ensembl
RefSeq Acc Id: ENST00000583369   ⟹   ENSP00000464321
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1774,748,652 - 74,768,582 (+)Ensembl
RefSeq Acc Id: NM_004252   ⟹   NP_004243
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381774,748,628 - 74,769,353 (+)NCBI
GRCh371772,744,751 - 72,765,499 (+)NCBI
Build 361770,256,373 - 70,277,089 (+)NCBI Archive
HuRef1768,155,124 - 68,175,866 (+)NCBI
CHM1_11772,809,571 - 72,830,338 (+)NCBI
T2T-CHM13v2.01775,640,506 - 75,661,228 (+)NCBI
Sequence:
Reference Protein Sequences
RefSeq Acc Id: NP_004243   ⟸   NM_004252
- UniProtKB: O43552 (UniProtKB/Swiss-Prot),   B3KY21 (UniProtKB/Swiss-Prot),   Q86WQ5 (UniProtKB/Swiss-Prot),   O14745 (UniProtKB/Swiss-Prot),   B2R6A3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000464117   ⟸   ENST00000581356
RefSeq Acc Id: ENSP00000464321   ⟸   ENST00000583369
RefSeq Acc Id: ENSP00000464982   ⟸   ENST00000413388
RefSeq Acc Id: ENSP00000262613   ⟸   ENST00000262613
Protein Domains
EBP50 C-terminal   PDZ

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-O14745-F1-model_v2 AlphaFold O14745 1-358 view protein structure

Promoters
RGD ID:6794406
Promoter ID:HG_KWN:27059
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_004252,   UC002JLN.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361770,256,106 - 70,256,606 (+)MPROMDB
RGD ID:7236225
Promoter ID:EPDNEW_H23858
Type:initiation region
Name:SLC9A3R1_1
Description:SLC9A3 regulator 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381774,748,628 - 74,748,688EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:11075 AgrOrtholog
COSMIC NHERF1 COSMIC
Ensembl Genes ENSG00000109062 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000262613 ENTREZGENE
  ENST00000262613.10 UniProtKB/Swiss-Prot
  ENST00000413388.2 UniProtKB/Swiss-Prot
  ENST00000581356.1 UniProtKB/TrEMBL
  ENST00000583369.5 UniProtKB/TrEMBL
Gene3D-CATH 2.30.42.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000109062 GTEx
HGNC ID HGNC:11075 ENTREZGENE
Human Proteome Map NHERF1 Human Proteome Map
InterPro EBP50_C-term UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  NHERF-1/NHERF-2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PDZ UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PDZ_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:9368 UniProtKB/Swiss-Prot
NCBI Gene 9368 ENTREZGENE
OMIM 604990 OMIM
PANTHER NA(+)/H(+) EXCHANGE REGULATORY COFACTOR NHE-RF1 UniProtKB/TrEMBL
  PDZ DOMAIN CONTAINING PROTEIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR14191:SF7 UniProtKB/Swiss-Prot
Pfam EBP50_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PDZ UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA35931 PharmGKB
PIRSF EBP50 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE PDZ UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART PDZ UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF50156 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt B2R6A3 ENTREZGENE, UniProtKB/TrEMBL
  B3KY21 ENTREZGENE
  J3QRA3_HUMAN UniProtKB/TrEMBL
  J3QRP6_HUMAN UniProtKB/TrEMBL
  NHRF1_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  O43552 ENTREZGENE
  Q86WQ5 ENTREZGENE
UniProt Secondary B3KY21 UniProtKB/Swiss-Prot
  O43552 UniProtKB/Swiss-Prot
  Q86WQ5 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2022-10-31 NHERF1  NHERF family PDZ scaffold protein 1  SLC9A3R1  SLC9A3 regulator 1  Symbol and/or name change 19259463 PROVISIONAL
2016-02-23 SLC9A3R1  SLC9A3 regulator 1    solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3 regulator 1  Symbol and/or name change 5135510 APPROVED
2012-03-27 SLC9A3R1  solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3 regulator 1  SLC9A3R1  solute carrier family 9 (sodium/hydrogen exchanger), member 3 regulator 1  Symbol and/or name change 5135510 APPROVED